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rs337847

From SNPedia

Orientationplus
Stabilizedplus
Make rs337847(A;A)
Make rs337847(A;G)
Make rs337847(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position78964065
GeneARSB
is asnp
is mentioned by
dbSNPrs337847
ebirs337847
HLIrs337847
Exacrs337847
Varsomers337847
Maprs337847
PheGenIrs337847
hapmaprs337847
1000 genomesrs337847
hgdprs337847
ensemblrs337847
gopubmedrs337847
geneviewrs337847
scholarrs337847
googlers337847
pharmgkbrs337847
gwascentralrs337847
openSNPrs337847
23andMers337847
23andMe allrs337847
SNP Nexus

SNPshotrs337847
SNPdbers337847
MSV3drs337847
GWAS Ctlgrs337847
GMAF0.1405
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19668339OA-icon.png]
Trait Hippocampal atrophy
Title Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease
Risk Allele
P-val 0.000007
Odds Ratio NR NR


GET Evidence
rs337847
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.851562
summary